Primary Device ID | 03701337606268 |
NIH Device Record Key | 6bd20e17-8f50-4a91-9542-6384d3b467f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEOSYS, IBS |
Version Model Number | G02 10181 |
Catalog Number | G02 10181 |
Company DUNS | 263616749 |
Company Name | IN2BONES |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03701337606268 [Primary] |
KDD | Kit, surgical instrument, disposable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
03701337606268 | NEOSYS SINGLE USE SET FOOT IBS 3.0C 16-18 |
03701337606244 | NEOSYS SINGLE USE SET FOOT IBS 2.5C 16-18 |
03701337606237 | NEOSYS SINGLE USE SET FOOT IBS 3.0C 16 |
03701337606220 | NEOSYS SINGLE USE SET FOOT IBS 2.5C 16 |